Purpose: This is a systematic review to evaluate the impact of various follow-up intensities and strategies on the outcome of patients after curative surgery for colorectal cancer. Methods: All randomized trials up to January 2007, comparing different follow-up intensities and strategies, were retrieved. Meta-analysis was performed by using the Forest plot review. Results: Eight randomized, clinical trials with 2,923 patients with colorectal cancer undergoing curative resection were reviewed. There was a significant reduction in overall mortality in patients having intensive follow-up (intensive vs. less intensive follow-up: 21.8 vs. 25.7 percent; P=0.01). Regular surveillance with serum carcinoembryonic antigen (P=0.0002) and colonoscopy (P=0.04) demonstrated a significant impact on overall mortality. However, cancer-related mortality did not show any significant difference. There was no significant difference in all-site recurrence and in local or distant metastasis. Detection of isolated local and hepatic recurrences was similar. Intensive follow-up detected asymptomatic recurrence more frequently (18.9 vs. 6.3 percent; P < 0.00001) and 5.91 months earlier than less intensive follow-up protocol; these were demonstrated with all investigation strategies used. Intensive surveillance program detected recurrences that were significantly more amenable to surgical reresection (10.7 vs. 5.7 percent; P=0.0002). The chance of curative reresection were significantly better with more intensive follow-up (24.3 vs. 9.9 percent; P=0.0001), independent of the investigation strategies used. Conclusions: Intensive follow-up after curative resection of colorectal cancer improved overall survival and reresection rate for recurrent disease. However, the cancer-related mortality was not improved and the survival benefit was not related to earlier detection and treatment of recurrent disease.
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Erasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, NetherlandsErasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, Netherlands
Mokhles, S.
Macbeth, F.
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Cardiff Univ, Wales Canc Trials Unit, Cardiff, S Glam, WalesErasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, Netherlands
Macbeth, F.
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Farewell, V.
Fiorentino, F.
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Imperial Coll, Div Surg & Canc, London, England
Imperial Coll, Imperial Coll Trials Unit, London, EnglandErasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, Netherlands
Fiorentino, F.
Williams, N. R.
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UCL, Fac Med Sci, Div Surg & Intervent Sci, Surg & Intervent Trials Unit, London, EnglandErasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, Netherlands
Williams, N. R.
Younes, R. N.
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Hosp Alemao Oswaldo Cruz, Oncol Ctr, Sao Paulo, BrazilErasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, Netherlands
Younes, R. N.
Takkenberg, J. J. M.
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Erasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, NetherlandsErasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, Netherlands
Takkenberg, J. J. M.
Treasure, T.
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UCL, Clin Operat Res Unit, 4 Taviton St, London WC1H 0BT, EnglandErasmus Univ, Med Ctr, Dept Cardiothorac Surg, Rotterdam, Netherlands
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Univ Penn Hlth Syst, Div Gastroenterol, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USAUniv Penn Hlth Syst, Div Gastroenterol, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
Lewis, JD
Kochman, ML
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Univ Penn Hlth Syst, Div Gastroenterol, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USAUniv Penn Hlth Syst, Div Gastroenterol, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
Kochman, ML
Hoops, TC
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Univ Penn Hlth Syst, Div Gastroenterol, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USAUniv Penn Hlth Syst, Div Gastroenterol, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA